Canonical Allele Identifier: PA2573165098
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1484169
ClinVar RCV Id: RCV002005597

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys997Arg
CA389046306
NM_000257.4:c.2990A>G